acquired abnormal hair pattern Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the distribution of hair growth that is acquired during the course of life. (Human Phenotype Ontology, HP_0011360)
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4 genes associated with the acquired abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CNBP CCHC-type zinc finger, nucleic acid binding protein
DMPK dystrophia myotonica-protein kinase
KDM5C lysine (K)-specific demethylase 5C
TP63 tumor protein p63